Job Description
Process Engineer Team Horizon is seeking a Process Engineer for a leading pharmaceutical company in Sligo. Joining team of 8, reporting to the NPI Technical Manager – team is divided into NPI/Tech Transfer and Manufacturing Support. Will be based at the Biologics site – parental drug product fill finish facility, supporting design, qualification, and management of single use technologies. Will interact with vendors/manufacturers and review drawings for connectors/filters etc. Will also work closely with manufacturing, ensuring Operators are trained in single use technologies. Will be involved in investigations/troubleshooting of issues as well as process improvements. Why you should apply: Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work. You enjoy working on exciting projects and want to work with a global manufacturing site in Sligo. What you will be doing: Process Engineer for Fill Finish Manufacturing site Leverage detailed understanding of aseptic fill finish manufacturing for design input into equipment commissioning and qualification. Responsible for single use design, onboarding, and qualification. Act as site representative on cross-site teams for standardization of single use assemblies and procedures. Work with supplier technical teams to maintain good relationship. Technical representative on site cross-functional team for design updates and introduction of new single use to site. Author of process flow diagrams for new product introductions / technology transfers. Responsible for aligning PFD between products and standardizing for NPI. Aligns with NPI Lead for product transfer on requirements for new products or process improvements. Technical SME for investigations, responsible for process improvements and monitoring of process efficiency. Author gap assessments, facility fit studies, process safety and risk assessments for NPI. Author scientific reports and technical documentation and presentations to document and communicate project status to internal and external stakeholders. Understand and ensure compliance with safety, regulatory and compliance expectations. Other duties as assigned. What you need to apply: Third level degree in Chemical Engineering, Bioprocess Engineering. 3-5 years’ experience in biopharmaceutical industry. Biologics experience with at scale manufacturing in fill finish facility in a technical role. Experience with new product introductions / technology transfers to fill finish manufacturing facility. Experience in single use technology. Experience in isolator technology. Experience in SAP / Trackwise. Single use Technology: design and qualification in drug product/Fill finish or drug substance is also applicable. Experience dealing with vendors. Operations or design background in single use technology and experience in onboarding single use into a facility. Ability to interact with Operations/Manufacturing on single use training/continuous improvement initiatives. #J-18808-Ljbffr